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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713243Generated: October 31, 2026

Allylamine → HCID 21090184, compound

https://huagongshe.com/reaction/1713243

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllylamineHCID 7853—
ReactantEthyl AcetateHCID 8857—
ReactantHCID 21090199HCID 21090199—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 21090184HCID 2109018441%

Reaction Steps

A mixture of methyl 3-[5-chloro-4-[(2,4-difluorobenzyl)oxy]-2-(methylsulfonyl)-6-oxopyrimidin-1(6H)-yl]-4-methylbenzoate (from Step 1) (3.02 g, 6.05 mmol), allyl amine (0.55 mL, 7.26 mmol), and DMAP (0.07 g, 0.61 mmol) in dioxane (8 mL) was stirred at ambient temperature overnight. Observed product and impurity (1:1 ratio). Added ethyl acetate (4 mL), cooled (0° C.) the reaction mixture, filtered the precipitate, and dried in vacuo to give the product as a white solid (1.17 g, 41%). 1H NMR (CD3OD/400 MHz) δ8.08 (m, 1H), 7.82 (s, 1H), 7.57 (m, 2H), 7.00 (t, 2H, J=8.8 Hz), 5.80 (m, 1H), 5.51 (m, 2H), 5.07 (m, 2H), 4.56 (s, 1H), 3.93 (m, 1H), 3.89 (s, 3H), 3.65 (s, 3H). ESHRMS m/z 476.1184 (M+H calculated for C23H21ClF2N3O4 requires 476.1183).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795271B2
Source datasetuspto-grants-2010_09
ORD IDord-3f1b9f8de56f49dfa558542067097a11
Source noteuspto-grants-2010_09